Chemistry of Dioxacyclanes: XI. Synthesis and Properties of Unsaturated Derivatives of 1,3-Dioxolanes
摘要:
1,3-Dioxolanes were synthesized by reactions of 3-cyclohexenecarboxaldehyde and 5-norbornene2-endo-carboxaldehyde with 1,2-ethanedithiol and 3-(2-propenyloxy)- and 3-propoxy-1,2-propanediols, as well as of propionaldehyde, benzaldehyde, and trichloroacetaldehyde with the latter two thiols. Dichlorocarbene addition, bromination, and epoxidation of the ring C=C were accomplished, and activity of the resulting products as dienophiles in Dield-Alder reactions was assessed.
Method for Producing Compound Containing BIS (Perfluoroalkylsulfonyl) Methyl Group and Salt Thereof, and Solid Electrolyte Membrane Produced Using Same
申请人:CENTRAL GLASS COMPANY, LIMITED
公开号:US20150266816A1
公开(公告)日:2015-09-24
[Problem] To provide a method for producing a compound having a bis(trifluoroalkanesulfonyl)methyl group, which is a compound having a high acidity degree and hydrophobicity and useful as a raw material compound for a resin, and a salt thereof in a simple manner.
[Solution] A method for producing a compound containing a bis(perfluoroalkylsulfonyl)methyl group and represented by the following formula and a salt of the compound.
(Rf represents a perfluoroalkyl group having 1 to 12 carbon atoms. A represents a monovalent organic group. Y represents a single bond or a C
1
-C
4
linear, C
3
-C
4
branched or C
3
-C
4
cyclic alkylene group wherein each of some or all of hydrogen atoms may be substituted with a fluorine atom, a chlorine atom, a bromine atom or an iodine atom and an ether bond or an ester bond may be contained.)
Efficient synthesis of acetals catalysed by rare earth chlorides
作者:Jean-Louis Luche、Andr� Luis Gemal
DOI:10.1039/c39780000976
日期:——
Rareearthchlorides are efficient catalysts for the acetalization of aldehydes.
稀土氯化物是醛缩醛化的有效催化剂。
Chemistry of Dioxacyclanes: XI. Synthesis and Properties of Unsaturated Derivatives of 1,3-Dioxolanes
作者:A. Kh. Kerimov
DOI:10.1023/b:rugc.0000025512.21009.9e
日期:2004.2
1,3-Dioxolanes were synthesized by reactions of 3-cyclohexenecarboxaldehyde and 5-norbornene2-endo-carboxaldehyde with 1,2-ethanedithiol and 3-(2-propenyloxy)- and 3-propoxy-1,2-propanediols, as well as of propionaldehyde, benzaldehyde, and trichloroacetaldehyde with the latter two thiols. Dichlorocarbene addition, bromination, and epoxidation of the ring C=C were accomplished, and activity of the resulting products as dienophiles in Dield-Alder reactions was assessed.